Pharmaron Clinical

Pharmaron Clinical is an integrated platform of clinical R&D services. It is composed of a Clinical Pharmacology Center, a Bioanalysis Science Center. We are devoted to providing one-stop clinical research and development services of high quality to customers around the world. Our services cover clinical pharmacology, clinical metabolism, clinical bioanalysis, regulatory affairs, medical affairs, clinical operations, biometrics, pharmacometrics, pharmacovigilance, site management services (SMO), subject recruitment, site start up (SSU), real world research (RWR), and medical device regulations. Pharmaron Clinical has built up a global all-in-one platform through continuous investment in our scientists and facility construction in China, the United Kingdom and the United States. Furthermore, we have established the expertise which allows the Pharmaron Clinical Service Platform to provide customers with more value-added services. We have set-up integrated metabolism study capability including “synthesis of 14C-labelled drug substance, clinical bed research and 14C-based metabolite analysis”. Based on profound understanding of the differences between preclinical and clinical research, we provide customers with more effective translational medicine services. In a long run, we will continue to focus on meeting customer needs, strengthen the construction of various technical platforms and platform integration and enrich the content of services, such that creating value for our partners and customers, and providing assistance for global customers to obtain approval by international regulatory agencies for innovative drugs to benefit patients.

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Locations

APAC
North America

Overview Accreditations

Therapeutic Areas

Cardiovascular
Central Nervous System (CNS)
Endocrinology
Gastroenterology
Oncology
Respiratory

Accreditations

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.

Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.

Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality of the targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.